Traxler v. Varady

12 Cal. App. 4th 1321, 16 Cal. Rptr. 2d 297, 93 Daily Journal DAR 1423, 93 Cal. Daily Op. Serv. 747, 1993 Cal. App. LEXIS 82
CourtCalifornia Court of Appeal
DecidedJanuary 29, 1993
DocketA053098
StatusPublished
Cited by11 cases

This text of 12 Cal. App. 4th 1321 (Traxler v. Varady) is published on Counsel Stack Legal Research, covering California Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Traxler v. Varady, 12 Cal. App. 4th 1321, 16 Cal. Rptr. 2d 297, 93 Daily Journal DAR 1423, 93 Cal. Daily Op. Serv. 747, 1993 Cal. App. LEXIS 82 (Cal. Ct. App. 1993).

Opinion

Opinion

STEIN, J.

Shortly after giving birth to her daughter in 1982, appellant, Sheri R. Traxler, received a blood transfusion. By 1988, when Sheri Traxler first learned that she, tragically, had become one of the approximately 600,000 women worldwide who are now afflicted with Acquired Immune *1326 Deficiency Syndrome (AIDS), the human immunodeficiency vims (HIV) had been identified and the risk of infection through blood transfusion discovered. Unable to regain her health, appellant seeks damages from defendants Robert Varady, M.D., James C. Heinrich, M.D., Chris Cammisa, M.D., Fairfield Medical Group, Inc., and NorthBay Medical Center (hereinafter, hospital) alleging that various negligent acts had caused her to receive the HIV-tainted blood transfusion. She appeals from a judgment in favor of all defendants, contending that the court erred by refusing to give requested jury instructions on negligence per se, informed consent and battery.

Facts

After a normal pregnancy under the care of Dr. Chris Cammisa, appellant was admitted to NorthBay Medical Center where Dr. Robert Varady delivered her baby. Since this was Dr. Varady’s first delivery at the NorthBay Medical Center, Dr. James Heinrich was designated as his “proctor.” After appellant gave birth to a normal baby girl by vaginal delivery, Dr. Varady examined the placenta and concluded that it was intact, meaning that no significant amount of placental tissue had been retained in the utems.

Two weeks later, appellant began severe hemorrhaging, was mshed to the hospital and signed a consent form authorizing a dilatation and curettage procedure (D&C). 1 Dr. Cammisa estimated that appellant had already lost approximately two pints of blood and suspected that a blood transfiision might be necessary. He ordered two units of blood to be held for appellant. Dr. Cammisa then performed the D&C and removed some “necrotic-appearing tissue.” Unexpectedly, appellant continued to hemorrhage. After consulting with Dr. Heinrich, Dr. Cammisa placed appellant under general anesthesia and performed a second D&C. Only a few blood clots, which did not explain why appellant continued to hemorrhage, were found.

In the recovery room Dr. Heinrich evaluated appellant’s condition. Her total documented blood loss during this period comprised approximately 30-40 percent of her total blood volume. His primary concern was that she could hemorrhage again at anytime. Renewed hemorrhaging had occurred in *1327 approximately 10 percent of his postpartum hemorrhage cases. If she were to bleed again, an emergency hysterectomy would probably have to be performed. Dr. Heinrich was concerned that in her weakened condition appellant could not tolerate such a procedure and there would not be enough time to transfuse her if she rehemorrhaged. In his judgment, appellant’s mental state was still compromised by the anesthesia and other medication she had been given, including Valium and codeine. After conferring with Dr. Cammisa, who concurred with his assessment, Dr. Heinrich ordered that appellant receive two units of blood.

In 1988, after being notified by the Irwin Memorial Blood Bank that she might have received HIV-infected blood, appellant tested positive for the presence of the HIV virus. It was undisputed at trial that in 1982 the HIV virus had not yet been identified and that the risk of receiving HIV-tainted blood through a transfusion was unknown.

Appellant’s theory of liability was that Dr. Varady negligently performed the delivery by failing to ensure that no placental tissue was retained; that his negligence caused her to hemorrhage. She further alleged that Dr. Heinrich ordered an unnecessary transfusion, to which she did not give her informed consent. A unanimous jury found no negligence on the part of any of the defendants.

Analysis

I.

Appellant contends the trial court erred in refusing to give her requested instruction on “negligence per se.”

Appellant’s requested instruction read as follows: “If you find that a party to this action violated Title 22, California [Code of Regulations] Sections 70213(a) and (d); 70231; 70233; 70235; 70703 ; 70706; 70706.2; 70707; 70747; 70749; 70751 (a)(h) and 70753,[ 2 ] the Statutes and code sections just read to you, and that such a violation was a legal cause of injury to another, you will find that such violation was negligence unless such party proves by a preponderance of the evidence that he did what might reasonably be expected of a person of ordinary prudence, acting under similar circumstances, who desired to comply with the law. In order to sustain such burden of proof, such party must prove by a preponderance of the evidence that he was faced with circumstances which prevented compliance or justified noncompliance with the statutes and codes.”

*1328 Appellant has abandoned any claim of error as to most of the subdivisions of title 22 listed in her proposed instruction. She now contends only that the court should have given her requested negligence per se instruction with respect to title 22, section 70223, subdivision (g), and section 70707. 3

A—Section 70223, Subdivision (g)

We conclude that the trial court correctly refused to give appellant’s requested instruction on section 70223, subdivision (g), because the elements set forth in Evidence Code section 669, defining when an alleged violation of statute or regulation supports a presumption of negligence per se, were not supported by the evidence. 4

Section 669 of the Evidence Code provides that: “(a) The failure of a person to exercise due care is presumed if: (1) He violated a. . . regulation of a public entity; (2) The violation proximately caused death or injury. . . ; (3) The death or injury resulted from an occurrence of the nature which the . . . regulation was designed to prevent; and (4) The person suffering the death or injury to his person . . . was one of the class of persons for whose protection the . . . regulation was adopted.” The burden is on the proponent of a negligence per se instruction to démonstrate that these elements are met. (Ronald M. v. White (1980) 112 Cal.App.3d 473, 477 [169 Cal.Rptr. 370].) The first and second elements of section 669, although normally questions of fact for the jury, may be resolved by the court as a matter of law where reasonable minds could not differ as to whether a violation of the regulation actually occurred or whether the violation proximately caused the plaintiff’s injuries. (Capolungo v. Bondi (1986) 179 Cal.App.3d 346, 354 [224 Cal.Rptr. 326]; Horn v. Oh (1983) 147 Cal.App.3d 1094, 1101-1102 [195 Cal.Rptr. 720].) The third and fourth elements of Evidence Code section 669 must be determined by the court as a matter of law.

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Bluebook (online)
12 Cal. App. 4th 1321, 16 Cal. Rptr. 2d 297, 93 Daily Journal DAR 1423, 93 Cal. Daily Op. Serv. 747, 1993 Cal. App. LEXIS 82, Counsel Stack Legal Research, https://law.counselstack.com/opinion/traxler-v-varady-calctapp-1993.